کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5136110 | 1494000 | 2017 | 6 صفحه PDF | دانلود رایگان |
- Anti-dipeptidyl peptidase IV obtained from Antarctic krill protein hydrolysate.
- Two anti-DPP-IV peptides were AP (IC50Â =Â 0.0530mg/mL) and IPA (IC50Â =Â 0.0370mg/mL).
- Docking model showed that both IPA and AP on DPP-IV formed stable docking complexes.
Dipeptidyl peptidase IV (DPP-IV) played an important role in blood glucose regulation. Inhibition of DPP-IV may improve glycemic control in diabetics by preventing the rapid breakdown of incretin hormones and prolonging their physiological action. In this study, Antarctic krill (Euphausia superba) protein was hydrolyzed using animal proteolytic enzymes. The hydrolysate was purified sequentially by ultrafiltration, gel filtration chromatography and reversed phase high-performance liquid chromatography (RP-HPLC). DPP-IV inhibitory activity of the fractions achieved from Antarctic krill protein was determined by DPP-IV screening reagent kit. Two purified peptides were identified by Xevo G2-XS QTof mass spectrometer (QTOF-MS). One peptide purified was Ala-Pro (AP) with IC50 values of 0.0530Â mg/mL, the other Ile-Pro-Ala (IPA) with IC50 values of 0.0370Â mg/mL. They both exhibited strong DPP-IV inhibitory activity. The molecular docking analysis revealed that DPP-IV inhibition by AP and IPA was mainly due to formation of a strong interaction surface force with the 91-96 and 101-105 amino acids of the DPP-IV. Our results suggested that the protein hydrolysate from Antarctic krill can be considered as a promising natural source of DPP-IV inhibitory peptides in the management of diabetes.
Journal: Journal of Chromatography B - Volume 1064, 1 October 2017, Pages 56-61